Article
How to diagnose H63D Syndrome Type-2
2023-03-20
Abstract excerpt
H63D Syndrome Type-2 is a complex genetic disorder with diverse manifestations, including erratic iron metabolism, micro-inflammatory cascades, neuropsychiatric issues, organ damage, and other rare multi-faceted symptoms. A comprehensive understanding of the pathophysiology underlying this condition is essential for accurate diagnosis, appropriate management, and the development of targeted therapeutic approaches....
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Identifiers and source
- Literature Corpus work
- 01f7dcc6-29a4-5095-90da-b5129ec4aaf2
- DOI
- 10.22541/au.167935461.12225452/v1
